TY - JOUR
T1 - Monolayer Vanadium-Doped Tungsten Disulfide
T2 - A Room-Temperature Dilute Magnetic Semiconductor
AU - Zhang, Fu
AU - Zheng, Boyang
AU - Sebastian, Amritanand
AU - Olson, David H.
AU - Liu, Mingzu
AU - Fujisawa, Kazunori
AU - Pham, Yen Thi Hai
AU - Jimenez, Valery Ortiz
AU - Kalappattil, Vijaysankar
AU - Miao, Leixin
AU - Zhang, Tianyi
AU - Pendurthi, Rahul
AU - Lei, Yu
AU - Elías, Ana Laura
AU - Wang, Yuanxi
AU - Alem, Nasim
AU - Hopkins, Patrick E.
AU - Das, Saptarshi
AU - Crespi, Vincent H.
AU - Phan, Manh Huong
AU - Terrones, Mauricio
N1 - Funding Information:
This work was mainly supported by the Air Force Office of Scientific Research (AFOSR) through Grant No. FA9550‐18‐1‐0072 and the NSF‐IUCRC Center for Atomically Thin Multifunctional Coatings (ATOMIC). Theory efforts were supported by the Two‐Dimensional Crystal Consortium (2DCC‐MIP), a National Science Foundation Materials Innovation Platform, through award DMR‐1539916. M.H.P. acknowledges support from the U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering under Award No. DE‐FG02‐07ER46438 and the VISCOSTONE USA under Award No. 1253113200. P.E.H. appreciates support from NSF Grant No. DMR EPM 2006231 and NSF I/UCRC on Multi‐functional Integrated System Technology (MIST) Center; IIP‐1439644, IIP‐1439680, IIP‐1738752, IIP‐1939009, IIP‐1939050, and IIP‐1939012. The authors are grateful to Jeff Shallenberger from Material Characterization Laboratory at Penn State for his assistance with XPS measurements and to Yin‐Ting Yeh and Ethan L. Kahn for helpful discussions.
Funding Information:
This work was mainly supported by the Air Force Office of Scientific Research (AFOSR) through Grant No. FA9550-18-1-0072 and the NSF-IUCRC Center for Atomically Thin Multifunctional Coatings (ATOMIC). Theory efforts were supported by the Two-Dimensional Crystal Consortium (2DCC-MIP), a National Science Foundation Materials Innovation Platform, through award DMR-1539916. M.H.P. acknowledges support from the U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering under Award No. DE-FG02-07ER46438 and the VISCOSTONE USA under Award No. 1253113200. P.E.H. appreciates support from NSF Grant No. DMR EPM 2006231 and NSF I/UCRC on Multi-functional Integrated System Technology (MIST) Center; IIP-1439644, IIP-1439680, IIP-1738752, IIP-1939009, IIP-1939050, and IIP-1939012. The authors are grateful to Jeff Shallenberger from Material Characterization Laboratory at Penn State for his assistance with XPS measurements and to Yin-Ting Yeh and Ethan L. Kahn for helpful discussions.
Publisher Copyright:
© 2020 The Authors. Published by Wiley-VCH GmbH
PY - 2020/12/16
Y1 - 2020/12/16
N2 - Dilute magnetic semiconductors (DMS), achieved through substitutional doping of spin-polarized transition metals into semiconducting systems, enable experimental modulation of spin dynamics in ways that hold great promise for novel magneto–electric or magneto–optical devices, especially for two-dimensional (2D) systems such as transition metal dichalcogenides that accentuate interactions and activate valley degrees of freedom. Practical applications of 2D magnetism will likely require room-temperature operation, air stability, and (for magnetic semiconductors) the ability to achieve optimal doping levels without dopant aggregation. Here, room-temperature ferromagnetic order obtained in semiconducting vanadium-doped tungsten disulfide monolayers produced by a reliable single-step film sulfidation method across an exceptionally wide range of vanadium concentrations, up to 12 at% with minimal dopant aggregation, is described. These monolayers develop p-type transport as a function of vanadium incorporation and rapidly reach ambipolarity. Ferromagnetism peaks at an intermediate vanadium concentration of ~2 at% and decreases for higher concentrations, which is consistent with quenching due to orbital hybridization at closer vanadium–vanadium spacings, as supported by transmission electron microscopy, magnetometry, and first-principles calculations. Room-temperature 2D-DMS provide a new component to expand the functional scope of van der Waals heterostructures and bring semiconducting magnetic 2D heterostructures into the realm of practical application.
AB - Dilute magnetic semiconductors (DMS), achieved through substitutional doping of spin-polarized transition metals into semiconducting systems, enable experimental modulation of spin dynamics in ways that hold great promise for novel magneto–electric or magneto–optical devices, especially for two-dimensional (2D) systems such as transition metal dichalcogenides that accentuate interactions and activate valley degrees of freedom. Practical applications of 2D magnetism will likely require room-temperature operation, air stability, and (for magnetic semiconductors) the ability to achieve optimal doping levels without dopant aggregation. Here, room-temperature ferromagnetic order obtained in semiconducting vanadium-doped tungsten disulfide monolayers produced by a reliable single-step film sulfidation method across an exceptionally wide range of vanadium concentrations, up to 12 at% with minimal dopant aggregation, is described. These monolayers develop p-type transport as a function of vanadium incorporation and rapidly reach ambipolarity. Ferromagnetism peaks at an intermediate vanadium concentration of ~2 at% and decreases for higher concentrations, which is consistent with quenching due to orbital hybridization at closer vanadium–vanadium spacings, as supported by transmission electron microscopy, magnetometry, and first-principles calculations. Room-temperature 2D-DMS provide a new component to expand the functional scope of van der Waals heterostructures and bring semiconducting magnetic 2D heterostructures into the realm of practical application.
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U2 - 10.1002/advs.202001174
DO - 10.1002/advs.202001174
M3 - Article
C2 - 33344114
AN - SCOPUS:85096652275
SN - 2198-3844
VL - 7
JO - Advanced Science
JF - Advanced Science
IS - 24
M1 - 2001174
ER -